Arrow-pushing Instructions NA Aromatic rings can be acylated to yield ketones by treatment with AlCl3 and an acid chloride. The reactive species is an electrophilic, resonance-stabilized acylium ion. Draw curved arrows to show the movement of electrons in this step of the mechanism. H3C CH3COCI AICI3 XT CI CH3 AICI 3 H3C-C=0 AICI4
Arrow-pushing Instructions NA Aromatic rings can be acylated to yield ketones by treatment with AlCl3 and an acid chloride. The reactive species is an electrophilic, resonance-stabilized acylium ion. Draw curved arrows to show the movement of electrons in this step of the mechanism. H3C CH3COCI AICI3 XT CI CH3 AICI 3 H3C-C=0 AICI4
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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![?!
CH3COCI
AICI 3
H3C
Aromatic rings can be acylated to yield ketones by treatment with AlCl3 and an acid chloride. The reactive species is an electrophilic, resonance-stabilized acylium ion.
Draw curved arrows to show the movement of electrons in this step of the mechanism.
Arrow-pushing Instructions
XI
لى
AICI 3
CH3
H3C-C=0
AICI4](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F0956b951-904a-4e8f-b73a-a0aa05e6cd9c%2Ff8f1a0d3-e029-40bb-a85b-7fdbc0078fb1%2Fov5fytj_processed.png&w=3840&q=75)
Transcribed Image Text:?!
CH3COCI
AICI 3
H3C
Aromatic rings can be acylated to yield ketones by treatment with AlCl3 and an acid chloride. The reactive species is an electrophilic, resonance-stabilized acylium ion.
Draw curved arrows to show the movement of electrons in this step of the mechanism.
Arrow-pushing Instructions
XI
لى
AICI 3
CH3
H3C-C=0
AICI4
![Draw a resonance structure, complete with all formal charges and lone (unshared) electron pairs, that shows the resonance interaction of the cyano with the ortho position
in benzonitrile.
O
CEN
benzonitrile
• You do not have to consider stereochemistry.
• Include all valence lone pairs in your answer.
• In cases where there is more than one answer, just draw one.
?](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F0956b951-904a-4e8f-b73a-a0aa05e6cd9c%2Ff8f1a0d3-e029-40bb-a85b-7fdbc0078fb1%2F8a190t_processed.png&w=3840&q=75)
Transcribed Image Text:Draw a resonance structure, complete with all formal charges and lone (unshared) electron pairs, that shows the resonance interaction of the cyano with the ortho position
in benzonitrile.
O
CEN
benzonitrile
• You do not have to consider stereochemistry.
• Include all valence lone pairs in your answer.
• In cases where there is more than one answer, just draw one.
?
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